We are testing a new system for linking grants to scientists.
The funding information displayed below comes from the
NIH Research Portfolio Online Reporting Tools and the
NSF Award Database.
The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
You can help! If you notice any innacuracies, please
sign in and mark grants as correct or incorrect matches.
Sign in to see low-probability grants and correct any errors in linkage between grants and researchers.
High-probability grants
According to our matching algorithm, Charles D. Cook is the likely recipient of the following grants.
Years |
Recipients |
Code |
Title / Keywords |
Matching score |
1998 — 1999 |
Cook, Charles D |
F31Activity Code Description: To provide predoctoral individuals with supervised research training in specified health and health-related areas leading toward the research degree (e.g., Ph.D.). |
Rat Strain Dependent Antinociception @ University of North Carolina Chapel Hill
DESCRIPTION: (Applicant's Abstract) Recent experiments indicate that Fischer 344, Long-Evans and Lewis rats vary in their sensitivity to the antinociceptive effects of low and intermediate efficacy mu opioids, as well as high efficacy mu opioids when tested in assays that employ relatively intense noxious stimuli. The proposed projects are designed to analyze further the fundamental differences in the responsiveness of various rat strains to the antinociceptive effects of opioid compounds. Two experimental manipulations, both aimed at challenging the mu opioid receptor system, will be evaluated in rats, using a warm-water (50, 52 and 56 degrees Celsius) tail-withdrawal procedure. Each of the proposed experiments will employ three rat strains and a series of mu opioids that vary (low, intermediate and high) in their intrinsic efficacy at the mu opioid receptor. In Experiment 1, the effects of mu opioids will be examined before and after the administration of the irreversible mu opioids antagonist beta-funaltrexamine (beta-FNA), whereas in Experiment 2 the ability of the opioid system to adapt to chronic exposure to morphine will be assessed. It is predicted that the rat strains most sensitive to the antinociceptive effects of mu opioids will be least sensitive to challenges with beta-FNA and chronic morphine. As such, the results of these experiments should provide critical information concerning the mu opioid receptor system and the resulting strain differences in responsiveness to mu opioids.
|
1 |